Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 89500570 | HCID 89500570 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 89500527 | HCID 89500527 | — |
Reaction Steps
To a solution of [5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester (77.5 mg, 0.240 mmol) and NaOAc (59.0 mg, 0.719 mmol) in MeOH (1 ml) was added 2-furaldehyde (0.020 ml, 23.0 mg, 0.240 mmol). The reaction mixture was degassed with Ar and stirred for 15 min at 100° C. in a microwave. After cooling to 0° C., NaBH4 (10.02 mg, 0.252 mmol) was added portionwise and stirring was continued at rt for 1 h. The reaction mixture was quenched with water and diluted with EtOAc. The phases were separated and the aq. layer was twice reextracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The resulting title compound was purified by FC (cyclohexane:EtOAc 100:0 to 80:20).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284284B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-83ef3cc1e16740d8ad3f34db97ab80c9 |
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| Source note | uspto-grants-2016_03 |
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